לוח משרות דרושים מדעים מדוייקים עבודה זמנית, לחיפוש זה נמצאו 12 משרות

You will be part of the Data Collection Group, a diverse team of Integration Engineers, Technical Data Managers, Data Analysts, and Product Managers. Our group is responsible for the entire data lifecycle - from initial requirement definition to the final delivery of high-quality data to our internal customers in Algorithm teams, Product, and Project Management. In this role, you will ensure our data is precise, reliable, and meets the specific needs of our development teams, in addition to analyzing, checking and building platforms for users to access data.
What will your job look like?
Partner with internal stakeholders (Algorithm and Product Managers) to define data needs and translate them into structured collection plans and catalogs.
Lead data projects from the planning stage through execution, coordinating with our driving teams, to final delivery.
Build and maintain clear dashboards using BI tools to monitor data quality, validity, and delivery progress in real time.
Perform deep-dive research into various data components to identify and resolve anomalies, gaps or bottlenecks in our data pipelines.
Improve processes by innovation and outside-the-box thinking, applying AI-driven tools to build creative MVPs and POCs that automate workflows and solve various challenges.
Implement high standards for data validation, proactively identify trends, and raise "red flags" to stakeholders when data quality drops.

We are seeking a highly motivated and qualified Analytical Chemist for a temporary maternity leave replacement position with a strong passion for laboratory work. As part of our CMC team, you will play a central role in the chemical characterization of our products by developing and implementing analytical methods to identify and quantify both known and novel plant-derived compounds.
You will work closely with multidisciplinary teams - including QA/QC, Regulatory Affairs, Tech, and Clinical - to support drug development activities and regulatory submissions, including FDA approval of inhalation technology.
Key Responsibilities:
Operate, maintain, and troubleshoot analytical instruments such as GC/MS, UPLC, and Karl Fischer titrators.
Perform routine and non-routine chemical analyses.
Develop, optimize, and validate analytical methods.
Write and execute protocols related to method development and validation.
Contribute to the preparation of regulatory documentation for drug development submissions.
Support ongoing and future research and development initiatives.
Collaborate effectively with cross-functional teams to advance project goals.